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  • About Us
    • Our Purpose
    • Our Strategy
    • What we do
    • Our Impact
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    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Support Calendar – What’s On
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Open Space
      • Group Counselling Programme
    • Recently diagnosed
    • Connect with Others
    • Support for 8-14 yrs ‘Turning Point’
    • Support for 14-25 yrs ‘Yes I Can’
    • Schools
    • Siblings
    • End of Life and Bereavement
  • AD Annual International Conference
    • Highlights from the Action Duchenne Conference 2025
    • Action Duchenne Annual International Conference 2025
  • News, Webinars and Blogs
    • News
    • Webinar Series 2026
    • Webinar recordings
    • Bite-Sized Duchenne Science Live
      • Facts about Duchenne muscular dystrophy
      • Signs and Symptoms of Duchenne Muscular Dystrophy
      • Diagnosis of Duchenne Muscular Dystrophy
      • Crucial Genetic Terminology
      • Genetics – Blueprint of Duchenne Muscular Dystrophy
      • How is Duchenne Muscular Dystrophy Inherited?
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SAVE THE DATE for the Action Duchenne Annual International Conference 2025

You are here: Home / SAVE THE DATE for the Action Duchenne Annual International Conference 2025

SAVE THE DATE for the Action Duchenne Annual International Conference 2025

We are excited to announce the date for the Action Duchenne Annual International Conference 2025!

Taking place on Friday 14th and Saturday 15th of November at Leonardo Hotel in Hinckley, we hope that you and your family will join us to make our 2025 event our best one yet! We will bring together individuals living with Duchenne and their families, patient experts, clinicians, healthcare professionals and equipment providers. Register your interest now to be a part of two days of learning, connection and support which will inspire and empower you wherever you are in your Duchenne journey. 

Our conference truly is a place for the whole family

With 20+ sessions over two days covering a huge variety of topics and bringing you the most up to date information, we’ll also have our professionally run creche for younger children, the HangOut for teens and our PitStop to offer time out and support for adults whenever they need it. 

Register Your Interest

Our Current Events

There are lots of ways we can support you and your family. Please find links to our online support groups , support for schools and to register for our newly launched webinar series. If you would like to talk to one of our Support Officers, please email: info@actionduchenne.org

Become an Action Duchenne Member

We need YOUR support so that we can continue to support those living with Duchenne muscular dystrophy. Find out how YOU could support us by becoming a valued member, making a donation or fundraising for us here.

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“Making contact with Action Duchenne provided a lifeline”: Find out why Ben Dolling decided to run the London Marathon dressed as a parrot! Harry was diagnosed with Duchenne muscular dystrophy in 2019 Ben and his wife have 3 children: a daughter in year 3 and a son in his first year of university and Harry, …

The Power of Shared Experience: “Honestly, it would’ve been a much harder road without having joined this group.”   

Action Duchenne have monthly online meet-ups for Duchenne dads, mums and grandparents, facilitated by our Family Support Officers and designed to enable connection with those who truly understand. A Duchenne diagnosis can often set people apart from the support systems they usually rely on. Our support groups mean you can meet people who know exactly …

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Action Duchenne
5th Floor, Mariner House
62 Prince Street
Bristol
BS1 4QD

07535 498 506
info@actionduchenne.org 

 

 

 

 

 

 

 

 

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